A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690357



Internal ID21212210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169667681..169667681hg38UCSC Ensembl
chr4:170588832..170588832hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809750
Supporting Variants
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690357
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.125


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